Validation Engineer

Dawar Consulting•Tucson, AZ

2d•Onsite

About The Position

We are seeking a proactive Validation Engineer with 1–3 years of experience in a regulated manufacturing environment such as medical devices, pharmaceuticals, or biotechnology. This on-site role focuses on process validation activities to ensure compliance with FDA, ISO, cGMP, and internal quality standards while supporting continuous improvement and operational excellence.

Requirements

Bachelor’s degree in Engineering, Life Sciences, or related field
1–3 years of experience in validation within a regulated manufacturing environment
Knowledge of process validation principles, verification techniques, and industry standards
Familiarity with FDA regulations, ISO standards, and cGMP requirements
Strong technical writing, analytical, and problem-solving skills
Excellent communication and cross-functional collaboration abilities

Nice To Haves

Medical device, biotech, or pharmaceutical industry experience
Experience supporting audits, CAPA activities, and process improvement initiatives
Familiarity with risk assessments and validation documentation practices

Responsibilities

Develop, write, review, and execute process validation and process verification protocols and reports
Conduct risk assessments and support validation strategies for new and existing manufacturing processes
Analyze and interpret validation data to ensure compliance with regulatory and internal quality requirements
Collaborate with Manufacturing, Quality, and Design Transfer teams to resolve validation issues and implement corrective actions
Support process optimization and continuous improvement initiatives to improve quality and efficiency
Ensure compliance with FDA, ISO, cGMP, and internal regulatory standards
Maintain validation documentation, traceability records, and audit-ready files
Provide training and guidance on validation processes, procedures, and compliance requirements